Naloxone regulates the differentiation of neural stem cells via a receptor-independent pathway.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2020 Apr

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The abilities of opioids to activate downstream signaling pathways normally depend on the binding between opioids and their receptors. However, opioids may also function in a receptor-independent manner, especially in neural stem cells (NSCs) in which the expression of opioid receptors and endogenous opioid agonists is low. When two opioids, morphine and naloxone, were used during the early stage of NSC differentiation, increased neurogenesis was observed. However, naloxone methiodide, a membrane impenetrable analog of naloxone, did not affect the NSC differentiation. The abilities of morphine and naloxone to facilitate neurogenesis were also observed in opioid receptor-knockout NSCs. Therefore, morphine and naloxone promote neurogenesis in a receptor-independent manner at least during the early stage. In addition, the receptor-independent functions of opioids were not observed in methylcytosine dioxygenase ten-eleven translocation 1 (Tet1) knockout NSCs. When the expression of opioid receptors increased and the expression of Tet1 decreased during the late stage of NSC differentiation, morphine, but not naloxone, inhibited neurogenesis via traditional receptor-dependent and miR181a-Prox1-Notch-related pathway. In summary, the current results demonstrated the time-dependent effects of opioids during the differentiation of NSCs and provided additional insight on the complex functions of opioids. © 2020 Federation of American Societies for Experimental Biology.

Citation

Jinlong Chen, Lining Liang, Yuan Li, Yixin Zhang, Mengdan Zhang, Tingting Yang, Fei Meng, Xiaowei Lai, Changpeng Li, Jingcai He, Meiai He, Qiaoran Xu, Qian Li, Ping-Yee Law, Horace H Loh, Duanqing Pei, Hao Sun, Hui Zheng. Naloxone regulates the differentiation of neural stem cells via a receptor-independent pathway. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 2020 Apr;34(4):5917-5930